List of variants in gene ARHGEF9 reported as uncertain significance for Autism spectrum disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001353921.2(ARHGEF9):c.1474G>A (p.Gly492Ser)	rs1365914320	0.00001
NM_001353921.2(ARHGEF9):c.16G>A (p.Gly6Ser)	rs2056441301
NM_001353921.2(ARHGEF9):c.889C>T (p.Arg297Cys)	rs2050115619

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